Name | 3-aminopiperidine dihydrochloride |
Synonyms | piperidin-3-amine 3-AMINOPIPERIDINEHCL 3-AMINOPIPERIDINEDIHCL 3-AMINOPIPERIDINE 2HCL 3-aminopiperidine hydrochloride piperidin-3-amine dihydrochloride 3-AMINOPIPERIDINE DIHYDROCHLORIDE 3-aminopiperidine dihydrochloride 3-Amino piptrdine dihydro chloride 3-AMINOPIPERIDINE PIPERIDIN-3-YLAMINE (3R)-piperidin-3-amine dihydrochloride |
CAS | 138060-07-8 |
EINECS | 630-778-2 |
InChI | InChI=1/C5H12N2.2ClH/c6-5-2-1-3-7-4-5;;/h5,7H,1-4,6H2;2*1H/t5-;;/m1../s1 |
Molecular Formula | C5H14Cl2N2 |
Molar Mass | 173.08 |
Melting Point | 230°C (dec.)(lit.) |
Boling Point | 241.9°C at 760 mmHg |
Flash Point | 100.1°C |
Water Solubility | Partly miscible in water. |
Solubility | Methanol (Sparingly), Water (Slightly) |
Vapor Presure | 0.028mmHg at 25°C |
Appearance | White to light yellow solid |
Color | Off-white to beige |
Storage Condition | Inert atmosphere,Room Temperature |
Sensitive | Hygroscopic |
MDL | MFCD00012773 |
Physical and Chemical Properties | Melting point 230°C (dec.) |
Use | This product is for scientific research only and shall not be used for other purposes. |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S37/39 - Wear suitable gloves and eye/face protection S36 - Wear suitable protective clothing. |
WGK Germany | 3 |
HS Code | 29333990 |
Hazard Note | Irritant |
overview | 3-aminoperidine hydrochloride is a key chiral intermediate for the synthesis of liragliptin and alogliptin for the treatment of type II diabetes. |
use | 3-aminopiperidine dihydrochloride is a white to white crystal, which is a key intermediate of two new diabetic drugs alogliptin and liptin, and is also a fine chemical intermediate of other pesticides and additives. |
preparation | ethyl 3-piperidinoate is used as the starting material, after D-tartaric acid: resolution, multiple crystallization, dissociation, and the upper benzyl group to prepare (R)N-benzyl -3-piperidinoate ethyl ester, the ester is hydrolyzed to produce acid, and the acid reacts with diphenyl azide phosphate, and rearrangements occur at the same time, (R)-1-N-benzyl-3-N-tert-butoxycarbonyl-aminopiperidine was prepared, and then (R)-3-aminopiperidine dihydrochloride was prepared after debenzylation and debutoxycarbonylation and salt formation. |